A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748855



Internal ID20524882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:94659432..94659505hg38UCSC Ensembl
chr7:94288744..94288817hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287139
Samples
Known GenesPEG10
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748855
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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